| Tag | Content |
|---|
EnhancerAtlas ID | HS051-10242 |
Organism | Homo sapiens |
Tissue/cell | Fetal_thymus |
Coordinate | chr16:27246620-27250160 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| RUNX3 | MA0684.1 | chr16:27249896-27249906 | TTTGCGGTTT | - | 6.02 | | STAT1 | MA0137.3 | chr16:27248693-27248704 | TTTCCAGGAAA | + | 6.62 | | Stat4 | MA0518.1 | chr16:27248693-27248707 | TTTCCAGGAAATGT | + | 6.41 |
|
| | Number of super-enhancer constituents: 26 | ID | Coordinate | Tissue/cell |
| SE_12229 | chr16:27241372-27250118 | CD3 | | SE_16720 | chr16:27245200-27250160 | CD4_Naive_Primary_8pool | | SE_17688 | chr16:27239262-27252268 | CD4p_CD25-_CD45RAp_Naive | | SE_18531 | chr16:27239895-27251967 | CD4p_CD25-_Il17-_PMAstim_Th | | SE_19311 | chr16:27242831-27252253 | CD4p_CD25-_Il17p_PMAstim_Th17 | | SE_20310 | chr16:27241177-27251921 | CD56 | | SE_22780 | chr16:27241026-27251783 | CD8_primiary | | SE_25739 | chr16:27242908-27251726 | DND41 | | SE_26358 | chr16:27245453-27247639 | Duodenum_Smooth_Muscle | | SE_26358 | chr16:27247957-27249687 | Duodenum_Smooth_Muscle | | SE_31983 | chr16:27246371-27247789 | Gastric | | SE_31983 | chr16:27247951-27250272 | Gastric | | SE_38139 | chr16:27245404-27256130 | HUVEC | | SE_39026 | chr16:27245617-27247711 | IMR90 | | SE_42906 | chr16:27245699-27252242 | Lung | | SE_44539 | chr16:27245785-27247737 | NHDF-Ad | | SE_44539 | chr16:27247814-27249742 | NHDF-Ad | | SE_45474 | chr16:27246490-27247805 | NHLF | | SE_46240 | chr16:27245810-27250148 | Osteoblasts | | SE_47840 | chr16:27246925-27247324 | Pancreas | | SE_47840 | chr16:27248561-27248973 | Pancreas | | SE_50190 | chr16:27242852-27247781 | Sigmoid_Colon | | SE_50190 | chr16:27247798-27257562 | Sigmoid_Colon | | SE_52565 | chr16:27241172-27250328 | Small_Intestine | | SE_56648 | chr16:27245721-27247766 | u87 | | SE_61927 | chr16:27232897-27250352 | Toledo |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 5 | Chromosome | Start | End |
| chr16 | 27247570 | 27247639 | | chr16 | 27248798 | 27249418 | | chr16 | 27249665 | 27249878 | | chr16 | 27248071 | 27249863 | | chr16 | 27247912 | 27248049 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH16I027228 | chr16 | 27240033 | 27259120 |
|
Enhancer Sequence | CTGGAAATAA ACAGACCAAA AAAAGGGGGG TGACCAGGGG GCCTCATCAA AAAAATGTAG 60
CTTGCTTGAA TCATTCCATC CCATCTCAAC GCAGGGGACA GCAACCCCAG ACATGGGTGG 120
AGGCTGCAGC CTCTTGGGTG AACGCCAATG CCACGTGGCT TCTTTCTTCC TGGAGTACTT 180
GGAAGACAAA CAGACAACAG ATGGAGGGCG TTGTGAGGCA GGAGGGCCAG GGAGATGCTA 240
TCTGCAACCA CGGAGGCTGC CGCGGGCTTC CTGTCTTTGC TCGCTGCCTC CTGATGAGAG 300
TCCCAATCAG CACCTTCAGC GCATTACTCA ATGATGTGCT CAGAGCCTGC GTGAGCTCCC 360
GCCGCACAAA CATCCTATCC CATCTCAGCC CTTCTATCGC ATCCCCAGTG CCCCGCGAGA 420
GGCCTCTGTC CCTGTATGTC CCCACACATC TTAGGTGGAG CTTTATTCCT TTCTCTTTTT 480
ATTCAATGTC GGGTTATCCT CACTTACATG CCAGGCTTGT GCTGGGTCCT GGGCTGGAAC 540
AGTAAGAATA ACAACAAACG GGGTGAGAAG GGTGGCTTGC AGCGAGCCCT CAGCATGGAG 600
AGGCCCTGTC CTGGGCACCT TTTGTCGTCA TGAATCCACC CTCCAGCAGC TCTCTGGGCA 660
CAGGGGAAGA GGCTGAGACG CAGAGAGGTG AACTGACTCG CCCAGAGTTG CACCACAAGG 720
CCGGGGCTTT GACTTCTCTG TCGCCCACCT CCCCTGGCCC TGCCAGCAGG ATGCTCACAG 780
CCCAGGGGCC ACCATCCAGG TCCATCAGTC TGAGGAGGGG GCACCCACAC TATTGCCGGG 840
GGCTCAGCTG AGGAGGACAG AGAGGCTGCG GTGAGGACAG GAGCCCGTGG CCGGGGACAG 900
CAGGGCCTTT CTCCTGTGGC ACCAGGAAGC CTCTGAGCAC TGGAAGCAGT GGAAGGACAT 960
GGCCAGCGTT GTGTCCCTTT TATGCTGTGA AACTTTTTTT TTTTTTTTTT TTTTTTTGAG 1020
ACAGAGTCTT GCTCTCGCCC TGGCTGGAGT GCAGTAGCAC AGTCTTGGCT CACTGCAACC 1080
TCCACCTCCC GGGTTCAAGC AGTTCTCCTG CCTTAGCCTC CCGAGGAGTT GAGATTACAG 1140
GCATGCACCA CCACACCCAG CTAATTTTTG TATTTTTAGT AGAGATGGGG TTTTACCATG 1200
TTGGCCAGGC TGGTCTCGAT CTCCTGACCT CAAGTGTTCC GCCCACCTCA GCTTCCCAAA 1260
GTGCTGGGAT TATAGGCGTG AGCCACCACG CCCAGCTTGT GCTGTGAAAC TTTTTAAAGC 1320
AAGAGTATGT ATTATTGTTT TCACTACTGT TTTTATGTAT TAAAATAAAT AATTTCAAAA 1380
GATTCATGCC TTAGAAAATC ATTCTGGAAA AAAAACTGCA AGAAAAAATG GACAATATGA 1440
TACATTCATG TGTGAAACAA AAACAGAACC AATGAAACAG TCCCACAGGA AAAGGCCCAG 1500
CAGGTTACCC ACTGGACTGA CGACCAAGGC CATCGCCAGG AAGGGACTAA ACGAAGGGTC 1560
ATCACAGGGC ACTCGTGCTG TATGTCTGTG TTTGATTTCT TATTAGACAG AGGCATTTCT 1620
AAGCTACCCG TACAACTCAA GATTCATAAA GTTAAAAAAA AAAACAACAG AAGATCATGC 1680
TGGTGACAAT GGAGGATGTG GCCGTGTGAA AGAGTCAAGG AAAACCCAGG CCAATGAGCT 1740
CTGTCAGAGG ATCAGACTGT GGGGCCCAGA AAAGCTGAGA ACAAAGCCCA GGGCAGTGAC 1800
ACTAATGTGC CATGCTCAGC GAGGAGCTAA TCTTCCCTTT CAGTTAAGTT TTTAAAAGGC 1860
AGTTTAAATT AAAAAGTAGT CATAGTAAGT GGGTGGAACA TGGATGTGGT GAGATCGTAA 1920
CATATGACAA TGACATCTGG CCTCGGCGGC TGGAGAGCAG GCATCAGGAG GGAGGCATGG 1980
CCTGACTTCC TGCCTCCATG CCCCTGCTCA CGGGCCCCTC CTTTCTGAAA ACTCCTCTCC 2040
CTCCACTGCG GCAGCCACCT TGGATGGCCT GTTTTTCCAG GAAATGTTCT CTTCTGCCCC 2100
CGGTGCTGTC TTCCTCTTCC ACAGCATGCA AGGCAGCTCT TTGCTGGCGT GGGAGCCGAG 2160
CTGTTCCGTA CCTGCCTGTG CCAGTGACTT GGCCAGACAC ACTTTTCCAC CCCCAAGGGG 2220
AGCCAACGCT GGGCAGCTCA GGTGCAAGAG GCCCAGACAT CAAAAAGCCT CGTTCAGTGC 2280
GGAGTGAGTG ACAGGAACCC TGTCCACCCA GTGTGACACT GGGGCAAGTC CCACCTCTCT 2340
GAAAGTGACA ATTCACATTT TCCACTAACG AGGCCCCTCC TGGGTATCAC TGAGAACAAT 2400
GTGCCCTGTG GGCAGATGAG AAGCATTCTG ATCTATTGGA CTTTCCAGAC ACCCCGTTGC 2460
AGGGAGGGAG CCAGCAGCCC TCTCTGCCCT TCCCCTCTCC ACACCACCTC TGGTTTGGCG 2520
TCCAGCCTCA TTTTTCAGAA ACCATGAATG TTTTGCTGTA TTTTCATCTG ACCAACCACT 2580
TCCTCCTACT GTACTCGCTC ACTGCACACA CCAGCCACTG CTTGGGCGCT CCCGTTCTCT 2640
CCGCTATCGC CCTCTTTCCT TCCACACGCT TCCTGCATCA GGGTCATGTC CACGATCTCC 2700
ATCGCTGACC CTGTAACTGT TTCTCACGGA GGCCCCGCGC CCTTGCAGCT CCTCTTAATC 2760
GTGACCTGAG AAGAAACTTC TCTTACACTC AGCACCCCCA AACCCTTCAA CTGACTCCTT 2820
TCAGCAGCAA CAGAGGTGGC GTGGTGGCAT GGGGCCAGAA GCAGAGGTGT GGGCTCTAGC 2880
CCATCCTGCC CTCCCGCTCT GTGGGGCCCT GCGTGAGCCT CTCCCCCACT TCTCATCTCT 2940
AACAGCCACA CACAGTCTCG CCTCCAGCCT CACACATGTC CAGAACCCTC TTCCCTCCCG 3000
CTTCTCTACC ACCACCCCTG GCTGGACCCC AGCCTCCTGA TCCTCTGGCA GCCTCCCGTA 3060
CAGGCCTTCC CCAACCAGAT AAGCTGCACT TCCCAGCTCT GTCCTCCCAT GGCAGCACTT 3120
CCTTCCTCAT CACGTGGCAC TCCAGTTACT GTGTCCAGCC GCCGCCCCAA GACAGGAGTC 3180
AGCTGGTGAC ACCTGCCAGC CCAGCAGCCA TGTCCCTCCC TAACGAGACC TTCGCCTTTT 3240
TTCTTTTTTT TTTTTTACAA TTGTCTTTCT CTTACATTTG CGGTTTTGGT GAGAGAATAA 3300
TTCCAGGTAT GATATTCAGG GAACCAGAAA GCAGAAAGCT GAAGGGACCA GAGATTAGGG 3360
CAGCCAGGAG TAGACAGAGA ACCCCTATCA GCCAGACACT CTCCCAATCT GAGCAAGGGA 3420
CAAAAGGAAG CTTGGAGGTG GCTCCAGCCC AGAAGCTACA GAGGGCCAGC TGCTCTGGCC 3480
ATGAGGTGAT GCCATGCTTC CTGCCTATCC CCAACTGTGC ACCTGGCCAC CAATGAGTCC 3540
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